2D CoP supported 0D WO3 constructed S-scheme for efficient photocatalytic hydrogen evolution

被引:72
作者
Li, Teng [1 ]
Guo, Xin [1 ]
Zhang, Lijun [1 ]
Yan, Teng [1 ]
Jin, Zhiliang [1 ]
机构
[1] North Minzu Univ, Sch Chem & Chem Engn, Ningxia Key Lab Solar Chem Convers Technol, Key Lab Chem Engn & Technol,State Ethn Affairs Co, Yinchuan 750021, Peoples R China
关键词
S-scheme heterojunction; Transition metal phosphide; Hydrogen evolution; WO < sub > 3 <; sub > nanoparticles; ELECTRON-HOLE SEPARATION; HETEROJUNCTION; WATER; NANOPARTICLES;
D O I
10.1016/j.ijhydene.2021.03.169
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
For heterojunction composite photocatalyst, intimate contact interface is the key to the carrier transfer separation conditions. Due to the interface contact, the electron transfer rate between catalysts can be increased during photocatalytic hydrogen production, therefore, we design the close contact of 0D/2D heterojunction, which greatly enhanced the photocatalytic hydrogen production activity of the composite catalyst. The composite catalyst WO3/CoP was obtained by simple high temperature in situ synthesis. Moreover, it was proved by photoelectric chemistry and fluorescence tests that appropriate conduction band and valence band locations of WO3 and CoP provided a favorable way for thermodynamic electron transfer. In addition, fluorescence results showed that WO3 load effectively promoted photoelectron-hole transfer and increased electron lifetime. The formation of S-scheme heterojunctions can make more efficient use of useful photo generated electrons and prevent the photogenerated electron-hole recombination of CoP itself, further promote the liveness of photocatalytic H2 evolution. Meanwhile, the study of Metal-organic frameworks (MOFs) materials further promoted the application of MOFs derivatives in the field of photocatalytic hydrogen evolution, and provided a reference for the rational design of composite catalysts for transition metal phosphide photocatalysts. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved. <comment>Superscript/Subscript Available</comment
引用
收藏
页码:20560 / 20572
页数:13
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